Mikami Yurie, Fujii Shinsuke, Kohashi Ken-Ichi, Yamada Yuichi, Moriyama Masafumi, Kawano Shintaro, Nakamura Seiji, Oda Yoshinao, Kiyoshima Tamotsu
Laboratory of Oral Pathology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, Higashi-ku, Fukuoka 812-8582, Japan.
Section of Maxillofacial Oncology, Division of Maxillofacial Diagnostic and Surgical Sciences, Faculty of Dental Science, Kyushu University, Higashi-ku, Fukuoka 812-8582, Japan.
Oncol Lett. 2018 Sep;16(3):3889-3894. doi: 10.3892/ol.2018.9115. Epub 2018 Jul 10.
Low-grade myofibroblastic sarcoma (LGMS) is a rare intermediate tumor, which rarely metastasizes and has myofibroblastic differentiation in various sites. It is particularly associated with the tongue in the head and neck region. The lack of any pathological features means it is difficult to make a conclusive diagnosis of LGMS. The immunohistochemical features and genomic rearrangements, including SS18-SSXs and MYH9-USP6s and the genetic mutations of cancer-associated genes, including APC, CTNNB1, EGFR, KRAS, PIK3CA and p53 were examined in a case of LGMS arising in the tip of the tongue. Immunohistochemically, the tumor cells were positive for alpha-smooth muscle actin and vimentin, as in previous reports. They demonstrated neither genomic rearrangements nor point mutations of cancer-associated genes. Although several tumor cells demonstrated intravascular invasion, the MIB-l labeling index of the cells was the same as the original lesion. To the best of our knowledge, this is the first case report of LGMS arising in the tip of the tongue with intravascular invasion.
低级别肌成纤维细胞肉瘤(LGMS)是一种罕见的中间型肿瘤,很少发生转移,可在多个部位出现肌成纤维细胞分化。它尤其与头颈部的舌部相关。缺乏任何病理特征意味着很难对LGMS做出确定性诊断。在一例起源于舌尖的LGMS病例中,检测了免疫组化特征和基因组重排,包括SS18 - SSXs和MYH9 - USP6s,以及癌症相关基因的基因突变,包括APC、CTNNB1、EGFR、KRAS、PIK3CA和p53。免疫组化显示,与之前的报道一样,肿瘤细胞α - 平滑肌肌动蛋白和波形蛋白呈阳性。它们既未显示基因组重排,也未显示癌症相关基因的点突变。尽管有几个肿瘤细胞显示血管内浸润,但这些细胞的MIB - 1标记指数与原发灶相同。据我们所知,这是首例起源于舌尖且伴有血管内浸润的LGMS病例报告。